Healthy Moms-Healthy Kids: Reducing Maternal Depression for Better Outcomes in Head Start Children
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT02145273|
Recruitment Status : Completed
First Posted : May 22, 2014
Last Update Posted : June 11, 2019
|Condition or disease||Intervention/treatment||Phase|
|Maternal Depression Parenting Behavior Health Interpersonal Relationships Goal Directed Behavior Child Behavior Child School Readiness||Behavioral: Interpersonal Psychotherapy for Depression -Group||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||208 participants|
|Intervention Model:||Parallel Assignment|
|Intervention Model Description:||There are 3 conditions that will be followed for up to 2 years: control, intervention and comparison. Randomization is by site. Half the sites are control half are intervention. all possible subjects are screened for depression. if the subject is depressed they are invited in to control or intervention based on site, all non depressed subjects are invited into the comparison.|
|Masking:||None (Open Label)|
|Official Title:||Healthy Moms-Healthy Kids: Reducing Maternal Depression for Better Outcomes in Head Start Children|
|Study Start Date :||September 2014|
|Actual Primary Completion Date :||September 2018|
|Actual Study Completion Date :||September 2018|
Subjects screen positive for depression and are offered a group Therapy intervention for depression: Interpersonal Psychotherapy for Depression Group.
Behavioral: Interpersonal Psychotherapy for Depression -Group
No Intervention: Control
Subjects screen positive for depression and are offered Treatment as usual: External referral.
No Intervention: comparison
Subjects screen negative for depression: no referral or intervention.
- Beck Depression Inventory [ Time Frame: At entry, completion of intervention, and every 6 months for 2 years ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02145273
|United States, California|
|Children's Institute, Inc.|
|Los Angeles, California, United States, 90026|
|University of Southern California School of Social Work|
|Los Angeles, California, United States, 90089|